Search research articles
Contact Us
Filters
Showing results (981-990 of 1,201) with videos related to
Page
of 121
Sort By:
Human Molecular Genetics
|
January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy
Artur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
Circulation
|
March 11, 1998
Prediction of indications for valve replacement among asymptomatic or minimally symptomatic patients with chronic aortic regurgitation and normal left ventricular performance
J S Borer, C Hochreiter, E M Herrold, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 11, 2011
Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration
Debarshi Mustafi, Brian M Kevany, Christel Genoud, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology
|
August 14, 2015
Shear stress blunts tubuloglomerular feedback partially mediated by primary cilia and nitric oxide at the macula densa
Lei Wang, Chunyu Shen, Haifeng Liu, et al.
Leukemia & Lymphoma
|
December 1, 1995
Molecular heterogeneity in childhood precursor B acute lymphoblastic leukemia with immunoglobulin heavy chain gene in germline configuration
J Roman Gomez, P Andres, M J Garcia, et al.
Investigative Ophthalmology & Visual Science
|
September 23, 2016
Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations
Samuel G Jacobson, David B McGuigan, Alexander Sumaroka, et al.
Hypertension (Dallas, Tex. : 1979)
|
May 23, 2001
Aortic root dilatation at sinuses of valsalva and aortic regurgitation in hypertensive and normotensive subjects: The Hypertension Genetic Epidemiology Network Study
V Palmieri, J N Bella, D K Arnett, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
October 16, 2002
Heritability of carotid artery structure and function: the Strong Heart Family Study
Kari E North, Jean W MacCluer, Richard B Devereux, et al.
The Journal of Chemical Physics
|
January 14, 2023
Modular mixing in plasmonic metal oxide nanocrystal gels with thermoreversible links
Jiho Kang, Zachary M Sherman, Hannah S N Crory, et al.
Ophthalmic Genetics
|
March 30, 2026
Bi-allelic pathogenic variants in <i>NR2E3</i> may be associated with a subtle enhanced S-cone syndrome phenotype
Alexander Hüther, Caroline L Sherman, Alexander Sumaroka, et al.
Page
of 121
Search research articles
Search
Showing results (981-990 of 1,201) with videos related to
Sort By:
Page
of 121
Human Molecular Genetics
|
January 20, 2011
Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy
Artur V Cideciyan, Rivka A Rachel, Tomas S Aleman, et al.
Circulation
|
March 11, 1998
Prediction of indications for valve replacement among asymptomatic or minimally symptomatic patients with chronic aortic regurgitation and normal left ventricular performance
J S Borer, C Hochreiter, E M Herrold, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 11, 2011
Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration
Debarshi Mustafi, Brian M Kevany, Christel Genoud, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology
|
August 14, 2015
Shear stress blunts tubuloglomerular feedback partially mediated by primary cilia and nitric oxide at the macula densa
Lei Wang, Chunyu Shen, Haifeng Liu, et al.
Leukemia & Lymphoma
|
December 1, 1995
Molecular heterogeneity in childhood precursor B acute lymphoblastic leukemia with immunoglobulin heavy chain gene in germline configuration
J Roman Gomez, P Andres, M J Garcia, et al.
Investigative Ophthalmology & Visual Science
|
September 23, 2016
Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations
Samuel G Jacobson, David B McGuigan, Alexander Sumaroka, et al.
Hypertension (Dallas, Tex. : 1979)
|
May 23, 2001
Aortic root dilatation at sinuses of valsalva and aortic regurgitation in hypertensive and normotensive subjects: The Hypertension Genetic Epidemiology Network Study
V Palmieri, J N Bella, D K Arnett, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
October 16, 2002
Heritability of carotid artery structure and function: the Strong Heart Family Study
Kari E North, Jean W MacCluer, Richard B Devereux, et al.
The Journal of Chemical Physics
|
January 14, 2023
Modular mixing in plasmonic metal oxide nanocrystal gels with thermoreversible links
Jiho Kang, Zachary M Sherman, Hannah S N Crory, et al.
Ophthalmic Genetics
|
March 30, 2026
Bi-allelic pathogenic variants in <i>NR2E3</i> may be associated with a subtle enhanced S-cone syndrome phenotype
Alexander Hüther, Caroline L Sherman, Alexander Sumaroka, et al.
Page
of 121